Evaluation of an Incontinence Product

Stopped early

Conditions studied: Incontinence

In brief

The purpose of this study is to determine if the sponsor's Incontinence Product reduces patient exposure time to a wet and/or soiled incontinence pad.

Key facts

Study ID

NCT03023072

Run by

Hill-Rom

People needed

9

Starts

2017-01-01

Expected to finish

2018-01-30

Last updated by the study team

2018-02-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• English speaking/reading adults, age ≥ 18 years
• Incontinent (fecal, urine, or dual incontinence)
• Patients with dual incontinence who require use of a fecal management system (but no urinary catheter)
• Absence of skin irritation, breakdown, and pressure injuries present in the buttocks, sacrum, and/or perineal areas at the time of enrollment; minor irritation may be acceptable at the discretion of the Study Investigator
• Willing and able to provide written informed consent or legal authorized representative is willing and able to provide written informed consent

You may not qualify if…

• Presence of skin irritation and/or breakdown including but not limited to IAD or pressure injuries present in the buttocks, sacrum, and/or perineal areas at the time of enrollment; minor irritation may be acceptable at the discretion of the study Investigator
• Require use of an absorbent undergarment (e.g. Depends) or catheter as the primary incontinence management strategy
• Is considered to be near death or requires hospice care

Where it is running

• Parkview Regional Medical Center — Fort Wayne, Indiana, United States

Full record on ClinicalTrials.gov

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